"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PPID"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 789176	NM_005038.3(PPID):c.529G>A (p.Val177Ile)	PPID (V177I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 711202	NM_005038.3(PPID):c.437_438del (p.His146fs)	PPID (H146fs)	Deletion (frameshift variant)	not provided	GLikely benign
Select item 791989	NM_005038.3(PPID):c.333+9G>C	PPID	Single nucleotide variant (intron variant)	not provided	GBenign

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